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Tundra lists 3 Bioequivalence Study clinical trials. Each listing includes eligibility criteria, study locations, and direct links to research sites in the Tundra directory.
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NCT03050164
Bioequivalence Study of Gefitinib Tablets Under Fasting Conditions
The study design is an Open-Label，Randomized, Single-Dose, 2-way Crossover Bioequivalence Study. During each session, the subjects will be administered a single dose of 250mg Gefitinib Tablet (one Gefitinib Tablet 250mg of Hunan Kelun or one Iressa® Tablet 250mg of AstraZeneca) under fasting conditions.
Gender: MALE
Ages: 18 Years - Any
Updated: 2026-05-26
NCT06549504
Bioequivalence Study of AG2202
The objective of this study is to evaluate the human bioequivalence of AG2202T and AG2202R.
Gender: All
Ages: 19 Years - Any
Updated: 2024-08-14
NCT06441916
Bioequivalence Study of Dabigatran Etexilate Capsules 150 mg in Healthy Thai Volunteers Under Fasting Conditions
The bioequivalence of Dabigatran Etexilate Capsules 150 mg to Boehringer Ingelheim's Pradaxa® will be assessed by a statistical comparison of various pharmacokinetic parameters derived from the plasma concentration-time curves of free dabigatran and total dabigatran.
Gender: All
Ages: 18 Years - 55 Years
Updated: 2024-06-06